US7727530B2 - Anti-cancer composition comprising proline or its derivatives and an anti-tumour antibody - Google Patents

Anti-cancer composition comprising proline or its derivatives and an anti-tumour antibody Download PDF

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US7727530B2
US7727530B2 US11/147,648 US14764805A US7727530B2 US 7727530 B2 US7727530 B2 US 7727530B2 US 14764805 A US14764805 A US 14764805A US 7727530 B2 US7727530 B2 US 7727530B2
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carcinoma
cell
proline
cancer
cells
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US20050276810A1 (en
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Zoser B. Salama
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401—Proline; Derivatives thereof, e.g. captopril
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4015—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising of proline or proline derivatives or their salts, esters, isomers or prodrugs together with an anti-cancer ligand, preferably an antibody directed to a tumour antigen.
  • the invention is also directed to the use of proline or proline derivatives or their salts, esters, isomers or prodrugs for the manufacture of a pharmaceutical composition for treating cancer and to a method of cancer treatment by administering said composition.
  • Cancer is a significant health problem in the world. Although advances have been made in cancer detection and treatment, no vaccine or other universally successful preventive or therapeutic method is currently available. Management of the disease currently relies on a combination of early diagnosis and aggressive treatment, which may include one or more of a variety of therapies such as surgery, radiotherapy, chemotherapy and hormone therapy. While such therapies provide benefit to many patients, a high mortality continues to be observed for many cancers. The development of improved anti-tumour agents would facilitate cancer prevention and treatment.
  • chemotherapeutic agents which possess little or no toxicity, which are inexpensive to obtain or manufacture, which are well tolerated by the patient, and which are easily administered would be a desirable addition to the therapeutic modalities currently available to the oncologist.
  • Agents that will selectively sensitize malignant tissue to allow lower doses of radiation or therapy to achieve the same therapeutic effect with less damage to healthy tissues are also desirable.
  • agents which prevent cancer from occurring or reoccurring are also desirable.
  • the present invention remedies these needs by providing such chemotherapeutic and sensitizing agents.
  • the technical problem underlying the present invention is to provide alternative or better modified compounds which demonstrate anti-cancer activity and from these compounds generate a pharmaceutical composition which could then be used as an anti-cancer treatment. It is also an object of the present invention to provide an anti-cancer composition which can be administered following the occurrence of multidrug resistance.
  • proline or a proline derivative e.g. cis-4-hydroxy-L-proline
  • an anti-cancer ligand preferably an antibody directed against an antigen (receptor) of a tumour cell
  • the combination compositions are effective in inhibiting survival and/or growth of cancer cells and/or for inhibiting undesirable cell growth in general.
  • This invention further provides pharmaceutical compositions, which contain a therapeutically effective amount of proline or proline derivatives or their salts, esters, isomers or prodrugs in combination with an anti-tumour antibody, and methods of treatment employing said compound combinations.
  • this invention relates to methods of treating cancer by administration of proline or a proline derivative, preferably cis-4-hydroxy-L-proline, 4-hydroxy-1-methyl-proline, 1-methyl-4-phenylamino-carbonyloxy-proline or 1-methyl-4-phenylamino-carbonyloxy-proline, or one of the salts, isomers, esters or prodrugs thereof in combination with an anti-tumour antibody preferably a monoclonal or a bispecific antibody.
  • proline derivatives which may be used according to the invention are cis-4-hydroxymethyl-L-proline, trans-4-hydroxymethyl-D-proline, trans-4-hydroxymethyl-L-proline, trans-4-methyl-L-proline and cis-3-Amino-L-proline or any of their corresponding salts.
  • Proline and its derivatives, as used according to the invention, are well known compounds which are commercially available.
  • the preferred proline derivatives used include esters, especially methyl, ethyl, propyl, isopropyl, butyl or isobutyl esters.
  • the antibodies used are in a preferred embodiment of the invention monoclonal antibodies and are selected from the group comprising Trastuzumab (Herceptin), Cetuximab, Rituximab, Avastatin or an EGFR-mAb.
  • the antibodies used are well known and commercially available antibodies directed to tumour antigens.
  • bispecific antibodies and/or multi-specific antibodies are also possible to use.
  • the invention is also directed to a method of treatment of cancer when multidrug resistance has occurred by administration of anti-tumour/anti-cancer drugs and/or the combination composition as described above.
  • the present invention provides a method for the combination of proline or its isoforms or derivatives thereof with antibodies which are directed against cancer-antigens and therefore have the ability to inhibit abnormal cell growth, in particular, to inhibit tumour cell growth and inhibit angiogenesis and the vascularization of endothelial cells.
  • kits for inhibiting abnormal cell growth comprising of the two active substances of the anti-cancer composition, especially the CHP, 4-hydroxy-1-methyl-proline or 1-methyl-4-phenylamino-carbonyloxy-proline, or the salt, ester, isomer or prodrug and the anti-cancer antibody.
  • the proline or any of its derivatives, or the salt, ester, isomer or prodrug is stored in a separate container to the anti-cancer antibody within the kit.
  • information on how to use each part of the kit By keeping the two active substances of the pharmaceutical composition separate, it is possible to administer the substances in different schemes (simultaneously or sequentially).
  • the invention further relates to a method of modification of tumour cell receptors, wherein the tumour cell is treated in vitro or in vivo with the combination composition of the invention or with proline or proline derivatives or their salts, esters, isomers or prodrugs.
  • FIG. 1 depicts proliferation activities of SW620 cells (in %) treated with varying concentrations of Cetuximab after pretreatment with CHP in comparison to untreated control(s).
  • FIG. 2 depicts proliferation activities of A431 cells (in %) treated with varying concentrations of Cetuximab after pretreatment with CHP in comparison to untreated control(s).
  • FIG. 3 shows proliferation activities of C205 cells (in %) treated with a direct combination of Cetuximab and CHP (the concentration of CHP was varied) in comparison to untreated control(s).
  • FIG. 4 shows the proliferation activities of SW620 cells (in %) treated with a direct combination of Cetuximab and CHP (the concentration of CHP was varied) in comparison to untreated control(s).
  • FIG. 5 shows the proliferation activities of C205 cells (in %) treated with a direct combination of Cetuximab and CHP (the concentration of Cetuximab was varied) in comparison to untreated control(s).
  • a “patient” for the purposes of the present invention includes both humans and other animals, particularly mammals, and other organisms. Thus the methods are applicable to both human therapy and veterinary applications.
  • the patient is a mammal, the most preferred being a human.
  • animal refers to an organism with a closed circulatory system of blood vessels and includes birds, mammals and crocodiles.
  • the term “animal” used here also includes human subjects.
  • angiogenesis refers to the generation of new blood vessels into cells, tissue, organs or tumours.
  • tumour refers to the process by which tumour cells are spread to distant parts of the body.
  • the term is also used herein to refer to a tumour that develops through the metastatic process.
  • contacting is used herein interchangeably with the following: combined with, added to, mixed with, passed over, incubated with, flowed over, etc.
  • compounds of present invention can be “administered” by any conventional method such as, for example, parenteral, oral, topical and inhalation routes as described herein.
  • the term “safe and effective amount” refers to the quantity of a component that is sufficient to yield a desired therapeutic response without undue adverse side effects (such as toxicity, irritation, or allergic response) commensurate with a reasonable benefit/risk ratio when used in the manner of this invention.
  • therapeutically effective amount is the amount of a compound of the present invention which is effective in yielding the desired therapeutic response. For example, an amount which is effective in delaying the growth of a cancer, either a sarcoma or lymphoma or which causes the cancer to shrink or not metastasize.
  • the specific amount which is safe and therapeutically effective will vary depending on such factors as the particular type of condition being treated, the physical condition of the patient, the type of mammal being treated, the duration of the treatment, the nature of concurrent therapy (if any), and the specific formulations employed and the structure of the compounds or its derivatives.
  • “An anti-angiogenic” amount refer to an amount of a compound or composition which is effective in depressing, suppressing or inhibiting angiogenesis or which results in the amelioration of symptoms associated with an angiogenic disease.
  • the desired result can be either a subjective relief of a symptom(s) or an objectively identifiable improvement in the recipient of the dosage, a decrease in the vascularization of endothelial cells or a decrease in the rate of angiogenesis as noted by a clinician or other qualified observer.
  • treating cancer refer generally to any improvement in the mammal having the cancer wherein the improvement can be ascribed to treatment with the compounds of the present invention.
  • the improvement can be either subjective or objective.
  • the patient may note improved vigour or vitality or decreased pain as subjective symptoms of improvement or response to therapy.
  • the clinician may notice a decrease in tumour size or tumour burden based on physical exam, laboratory parameters, tumour markers or radiographic findings.
  • Some laboratory obtained results which the clinician may observe to check for any response to therapy include normalization of tests such as white blood cell count, red blood cell count, platelet count, erythrocyte sedimentation rate, and various enzyme levels.
  • the clinician may observe a decrease in a detectable tumour marker(s).
  • other tests can be used to evaluate objective improvement such as sonograms, nuclear magnetic resonance testing and positron emissions testing.
  • “Inhibiting the growth of tumour cells” can be evaluated by any accepted method of measuring whether growth of the tumour cells has been slowed or diminished. This includes direct observation and indirect evaluation such as subjective symptoms or objective signs as discussed above.
  • compositions of the invention are administered to cells.
  • administered is the administration of a therapeutically effective dose of the candidate agents of the invention to a cell either in cell culture or in a patient.
  • therapeutically effective dose is a dose that produces the effects for which it is administered. The exact dose will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques. As is known in the art, adjustments for systemic versus localized delivery, age, body weight, general health, sex, diet, time of administration, drug interaction and the severity of the condition may be necessary, and will be ascertainable with routine experimentation by those skilled in the art.
  • cells is almost any cell in which mitosis or meiosis can be altered.
  • the present invention relates to the use of proline or proline derivatives or their salts, esters, isomers or prodrugs and anti-cancer ligands (preferably antibodies) for the manufacturing of a pharmaceutical composition for the treatment of a cell proliferative disorder.
  • the pharmaceutical composition of the invention optionally comprises of one or more pharmaceutically acceptable adjuvants, excipients, carriers, buffers, diluents and/or customary pharmaceutical auxiliary substances.
  • the combination-composition of the invention is administered in a pharmaceutically acceptable formulation.
  • the present invention pertains to any pharmaceutically acceptable formulations, such as synthetic or natural polymers in the form of macromolecular complexes, nanocapsules, microspheres, or beads, and lipid-based formulations including oil-in-water emulsions, micelles, mixed micelles, synthetic membrane vesicles, and resealed erythrocytes.
  • the pharmaceutically acceptable formulation used in the method of the invention can comprise additional pharmaceutically acceptable carriers and/or excipients.
  • a pharmaceutically acceptable carrier includes any and all solvents, dispersion media, coatings, antibacterial and anti fungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible.
  • the carrier can be suitable for injection into the blood.
  • Excipients include pharmaceutically acceptable stabilizers and disintegrants.
  • the pharmaceutically acceptable formulations comprise lipid-based formulations. Any of the known lipid-based drug delivery systems can be used in the practice of the invention.
  • multivesicular liposomes can all be used so long as a sustained release rate of the encapsulated combination-composition of the invention can be established.
  • the lipid-based formulation can be a multivesicular liposome system.
  • the composition of the synthetic membrane vesicle is usually a combination of phospholipids, usually in combination with steroids, especially cholesterol. Other phospholipids or other lipids may also be used. Examples of lipids useful in synthetic membrane vesicle production include phosphatidylglycerols, phosphatidylcholines, phosphatidylserines, phosphatidyl-ethanolaminos, sphingolipids, cerebrosides, and gangliosides.
  • phospholipids including egg phosphatidylcholine, dipalmitoylphosphatidylcholine, distearoylphosphatidylcholine, dioleoylphosphatidylcholine, dipalmitoylphosphatidylglycerol, and dioleoylphosphatidylglycerol are used.
  • the composition containing the combination-composition of the invention may be incorporated or impregnated into a bioabsorbable matrix.
  • the matrix may be comprised of the said biopolymer.
  • a suitable biopolymer for the present invention can include also one or more macromolecules selected from the group consisting of collagen, elastin, fibronectin, vitronectin, laminin, polyglycolic acid, hyaluronic acid, chondroitin sulphate, dermatan sulphate, heparin sulphate, heparin, fibrin, cellulose, gelatine, polylysine, echinonectin, entactin, thrombospondin, uvomorulin, biglycan, decorin, and dextran.
  • the formulation of these macromolecules into a biopolymer is well known in the art.
  • the therapeutic composition is not immunogenic when administered to a human patient for therapeutic purposes.
  • the therapeutic composition of the present invention can include pharmaceutically acceptable salts of the components therein.
  • Pharmaceutically acceptable salts include the acid addition salts that are formed with inorganic acids such as hydrochloric or phosphoric acids, or such organic acids as acetic, tartaric, mandelic and the like. Salts formed with the free carboxyl groups of the proline and the proline derivatives can also be derived from inorganic bases such as sodium, potassium, ammonium, calcium or ferric hydroxides, and such organic bases as isopropylamine, trimethylamino, 2-ethylamino ethanol, histidine, procaine and the like. Physiologically tolerable carriers are well known in the art.
  • Exemplary liquid carriers are sterile aqueous solutions which contain no materials in addition to the active ingredients and water, or contain a buffer such as sodium phosphate at a physiological pH value, in a physiological amount of saline or both, for example phosphate-buffered saline. Further still, aqueous carriers can contain more than one buffer salt, as well as salts such as sodium and potassium chlorides, dextrose, propylene glycol, polyethylene glycol and other solutes. Liquid compositions can also contain liquid phases in addition to and to the exclusion of water. Exemplary examples of such additional liquid phases include glycerine, vegetable oils such as cottonseed oil, organic esters such as ethyl oleate, and water-oil emulsions.
  • a therapeutic composition contains a composition of the present invention, typically an amount of at least 0.1 weight percent of composition per weight of total therapeutic composition.
  • a weight percent is a ratio by weight of composition of the invention to total composition.
  • 0.1 weight percent is 0.1 grams of proline, isomers, salts and fragments thereof together with the anti-cancer ligand per 100 grams of total composition.
  • pharmaceutically acceptable salt refers to those salts of compounds which retain the biological effectiveness and properties of the free bases and which are obtained by reaction with inorganic acids such as hydrochloric acid, hydrobromic acid, sulphuric acid, nitric acid, phosphoric acid, methanesulphonic acid, ethanesulphonic acid, ptoluenesulphonic acid, salicylic acid and the like.
  • Pharmaceutically acceptable salts include alkali metal salts, such as sodium and potassium, alkaline earth salts and ammonium salts.
  • composition containing the active ingredient may be in a form suitable for oral use, for example, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs.
  • Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavouring agents, colouring agents and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets.
  • excipients may be for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example corn starch, or alginic acid; binding agents, for example starch, gelatine or acacia, and lubricating agents, for example magnesium stearate, stearic acid or talc.
  • the tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.
  • a time delay material such as glyceryl monostearate or glyceryl distearate may be employed.
  • a pharmaceutical composition may also, or alternatively, contain one or more drugs, which may be linked to a modulating agent or may be free within the composition. Virtually any drug may be administered in combination with a modulating agent as described herein, for a variety of purposes as described below.
  • Examples of types of drugs that may be administered with a modulating agent include analgesics, anaesthetics, antianginals, antifungals, antibiotics, anti-cancer drugs (e.g., taxol or mitomycin C), anti-inflammatories (e.g., ibuprofen and indomethacin), anthelmintics, antidepressants, antidotes, antiemetics, antihistamines, antihypertensives, antimalarials, antimicrotubule agents (e.g., colchicine or vinca alkaloids), antimigraine agents, antimicrobials, antiphsychotics, antipyretics, antiseptics, anti-signalling agents (e.g., protein kinase C inhibitors or inhibitors of intracellular calcium mobilization), antiarthritics, antithrombin agents, antituberculotics, antitussives, antivirals, appetite suppressants, cardioactive drugs, chemical dependency drugs, cathartics,
  • Formulations for oral use may also be presented as hard gelatine capsules where in the active ingredient is mixed with an inert solid diluent, for example calcium carbonate, calcium phosphate or kaolin, or as soft gelatine capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.
  • an inert solid diluent for example calcium carbonate, calcium phosphate or kaolin
  • an oil medium for example peanut oil, liquid paraffin or olive oil.
  • Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions.
  • excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxy-propylmethylcellulose, sodium alginate polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally occurring phosphatide, for example lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such a polyoxyethylene with partial esters derived from fatty acids and hexitol anhydrides, for example polyoxyethylene sorbitan monooleate.
  • suspending agents for example sodium carboxymethylcellulose, methylcellulose,
  • the aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, p-hydroxybenzoate, one or more colouring agents, one or more flavouring agents, and one or more sweetening agents, such as sucrose or saccharin.
  • preservatives for example ethyl, or n-propyl, p-hydroxybenzoate, one or more colouring agents, one or more flavouring agents, and one or more sweetening agents, such as sucrose or saccharin.
  • Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, for example arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin.
  • the oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set forth above, and flavouring agents may be added to provide a palatable oral preparation. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
  • Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives.
  • a dispersing or wetting agent, suspending agent and one or more preservatives Suitable dispersing or wetting agents and suspending agents are exemplified, for example sweetening, flavouring and colouring agents, may also be present.
  • the pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions.
  • the oily phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these.
  • Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soya bean, lecithin, and esters/partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate.
  • the emulsions may also contain sweetening and flavouring agents.
  • Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain demulcent, preservatives, flavouring agents and colouring agents.
  • the pharmaceutical compositions may be in the form of a sterile injectable aqueous or oleagenous suspension. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned above.
  • the sterile injectable preparation may also be in a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example as absolution in 1,3-butane diol.
  • Suitable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid find use in the preparation of injectables.
  • the active substances of the present invention are mixed with a pharmaceutically acceptable carrier or diluent in accordance with routine procedures.
  • Therapeutic formulations will be administered by intravenous infusion or by subcutaneous injection.
  • the formulations can also contain, if desired, other therapeutic agents.
  • Dosage levels of the order of from about 0.05 mg to about 140 mg per kilogram of body weight per: day are useful in the treatment of the above-indicated conditions (about 2.5 mg to about 7 g per patient per day).
  • inflammation may be effectively treated by the administration of from about 0.01 to 50 mg of the compound per kilogram of body weight per day (about 0.5 mg to about 3.5 g per patient per day).
  • the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • a formulation intended for the oral administration of humans may vary from about 5 to about 95% of the total composition.
  • Dosage unit forms will generally contain between from about 1 mg to about 500 mg of active ingredient.
  • the specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet time of administration, route of administration, rate of excretion, drug combination and the severity of the particular disease undergoing therapy.
  • the dose effective amount of compounds according to the invention will vary depending upon factors including the particular compound, toxicity, and inhibitory activity, the condition treated, and whether the compound is administered alone or with other therapies. Typically a dose effective amount will range from about 0.0001 mg/kg to 1500 mg/kg, more preferably 1 to 1000 mg/kg, more preferably from about 1 to 150 mg/kg of body weight, and most preferably about 50 to 100 mg/kg of body weight.
  • the invention relates also to a process or a method for the treatment of the abovementioned pathological conditions.
  • the compounds of the present invention can be administered prophylactically or therapeutically, preferably in an amount that is effective against the mentioned disorders, to a warm-blooded animal, for example a human, requiring such treatment, the compounds preferably being used in the form of pharmaceutical compositions.
  • Formulation of pharmaceutically-acceptable excipients and carrier solutions is well-known to those of skill in the art, as is the development of suitable dosing and treatment regimens for using the particular compositions described herein in a variety of treatment regimens, including e.g., oral, parenteral, intravenous, intranasal, and intramuscular administration and formulation.
  • compositions disclosed herein may be delivered via oral administration.
  • these compositions may be formulated with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard- or soft-shell gelatine capsule, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet.
  • the active compounds may even be incorporated with excipients and used in the form of ingestible tablets, buccal tables, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.
  • the tablets, troches, pills, capsules and the like may also contain the following: a binder, as gum tragacanth, acacia, cornstarch, or gelatine; excipients, such as dicalcium phosphate; a disintegrating agent, such as corn starch, potato starch, alginic acid and the like; a lubricant, such as magnesium stearate; and a sweetening agent, such as sucrose, lactose or saccharin may be added or a flavouring agent, such as peppermint, oil of wintergreen, or cherry flavouring.
  • a binder as gum tragacanth, acacia, cornstarch, or gelatine
  • excipients such as dicalcium phosphate
  • a disintegrating agent such
  • the dosage unit form When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar, or both.
  • a syrup of elixir may contain the active compound sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and a flavouring, such as cherry or orange flavour.
  • any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed.
  • the active compounds may be incorporated into sustained-release preparation and formulations.
  • these formulations contain at least 0.1% of the active compound of the invention or more, although the percentage of the active ingredient(s) may, of course, be varied and may conveniently be between about 1 or 2% and about 60% or 70% or more of the weight or volume of the total formulation.
  • the amount of active compound(s) in each therapeutically useful composition may be prepared is such a way that a suitable dosage will be obtained in any given unit dose of the compound.
  • Factors such as solubility, bioavailability, biological half-life, route of administration, product shelf life, as well as other pharmacological considerations will be contemplated by one skilled in the art of preparing such pharmaceutical formulations, and as such, a variety of dosages and treatment regimens may be desirable.
  • compositions of the present invention may alternatively be incorporated with one or more excipients in the form of a mouthwash, dentifrice, buccal tablet, oral spray, or sublingual orally-administered formulation.
  • a mouthwash may be prepared incorporating the active ingredient in the required amount in an appropriate solvent, such as a sodium borate solution (Dobell's Solution).
  • the active ingredient may be incorporated into an oral solution such as one containing sodium borate, glycerine and potassium bicarbonate, or dispersed in a dentifrice, or added in a therapeutically-effective amount to a composition that may include water, binders, abrasives, flavouring agents, foaming agents, and humectants.
  • the compositions may be fashioned into a tablet or solution form that may be placed under the tongue or otherwise dissolved in the mouth.
  • compositions disclosed herein parenterally, intravenously, intramuscularly, or even intraperitoneally.
  • Solutions of the active compounds as free bases or as pharmacologically acceptable salts may be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose.
  • Dispersions may also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.
  • the pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions.
  • the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi.
  • the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and/or vegetable oils.
  • Proper fluidity may be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • a coating such as lecithin
  • surfactants for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars or sodium chloride.
  • Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminium monostearate and gelatine.
  • aqueous solutions For parenteral administration in an aqueous solution, for example, the solution should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose.
  • a sterile aqueous medium that can be employed will be known to those of skill in the art in light of the present disclosure.
  • one dosage may be dissolved in 1 ml of isotonic NaCl solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion. Some necessary variation in the dosage will occur depending on the condition of the subject being treated. The person responsible for administration will, in any event, determine the appropriate dose for the individual subject.
  • preparations should meet sterility, pyrogenicity, and the general safety and purity standards as required by national or regional offices of biologics standards.
  • Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above.
  • the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • compositions disclosed herein may be formulated in a neutral or salt form.
  • Pharmaceutically-acceptable salts include the acid addition salts (formed with the free amino groups of the protein) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, histidine, procaine and the like.
  • solutions Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective.
  • the formulations are easily administered in a variety of dosage forms such as injectable solutions, drug-release capsules, and the like.
  • carrier includes any and all solvents, dispersion media, vehicles, coatings, diluents, antibacterial and antifungal agents, isotonic and absorption delaying agents, buffers, carrier solutions, suspensions, colloids, and the like.
  • carrier includes any and all solvents, dispersion media, vehicles, coatings, diluents, antibacterial and antifungal agents, isotonic and absorption delaying agents, buffers, carrier solutions, suspensions, colloids, and the like.
  • the use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions.
  • compositions that do not produce an allergic or similar untoward reaction when administered to a human.
  • pharmaceutically-acceptable refers to molecular entities and compositions that do not produce an allergic or similar untoward reaction when administered to a human.
  • aqueous composition that contains a protein as an active ingredient is well understood in the art.
  • injectables either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection can also be prepared.
  • the preparation can also be emulsified.
  • the pharmaceutical compositions may be delivered by intranasal sprays, inhalation, and/or other aerosol delivery vehicles.
  • intranasal sprays inhalation, and/or other aerosol delivery vehicles.
  • delivery of drugs using intranasal microparticle resins and lysophosphatidylglycerol compounds are also well-known in the pharmaceutical arts.
  • the inventors contemplate the use of liposomes, nanocapsules, microparticles, microspheres, lipid particles, vesicles, and the like, for the introduction of the compositions of the present invention into suitable host cells.
  • the compositions of the present invention may be formulated for delivery either encapsulated in a lipid particle, a liposome, a vesicle, a nanosphere, or a nanoparticle or the like.
  • Such formulations may be preferred for the introduction of pharmaceutically-acceptable formulations of the combination-composition or constructs disclosed herein.
  • the formation and use of liposomes is generally known to those of skill in the art. Recently, liposomes were developed with improved serum stability and circulation half-times (Gabizon and Papahadjopoulos, 1988). Further, various methods of liposome and liposome like preparations as potential drug carriers have been reviewed (Takakura, 1998; Chandran et al., 1997; Margalit, 1995; U.S. Pat. Nos. 5,567,434; 5,552,157; 5,565,213; 5,738,868 and 5,795,587, each specifically incorporated herein by reference in its entirety).
  • an important determinant in entrapping compounds is the physicochemical properties of the compound itself. Polar compounds are trapped in the aqueous spaces and nonpolar compounds bind to the lipid bilayer of the vesicle. Polar compounds are released through permeation or when the bilayer is broken, but nonpolar compounds remain affiliated with the bilayer unless it is disrupted by temperature or exposure to lipoproteins. Both types show maximum efflux rates at the phase transition temperature.
  • Liposomes interact with cells via four different mechanisms: endocytosis by phagocytic cells of the reticuloendothelial system such as macrophages and neutrophils; adsorption to the cell surface, either by non-specific weak hydrophobic or electrostatic forces, or by specific interactions with cell-surface components; fusion with the plasma cell membrane by insertion of the lipid bilayer of the liposome into the plasma membrane with simultaneous release of liposomal contents into the cytoplasm; and by transfer of liposomal lipids to cellular or subcellular membranes, or vice versa, without any association of the liposome contents. It often is difficult to determine which mechanism is operative and more than one may operate at the same time.
  • liposomes The fate and disposition of intravenously injected liposomes depend on their physical properties, such as size, fluidity, and surface charge. They may persist in tissues for hours or days, depending on their composition, and half lives in the blood range from minutes to several hours. Larger liposomes, such as MLVs and LUVs, are taken up rapidly by phagocytic cells of the reticuloendothelial system, but physiology of the circulatory system restrains the exit of such large species at most sites. They can exit only in places where large openings or pores exist in the capillary endothelium, such as the sinusoids of the liver or spleen. Thus, these organs are the predominate site of uptake.
  • MLVs and LUVs are taken up rapidly by phagocytic cells of the reticuloendothelial system, but physiology of the circulatory system restrains the exit of such large species at most sites. They can exit only in places where large openings or pores exist in the capillary
  • SUVs show a broader tissue distribution but still are sequestered highly in the liver and spleen. In general, this in vivo behaviour limits the potential targeting of liposomes to only those organs and tissues accessible to their large size. These include the blood, liver, spleen, bone marrow, and lymphoid organs.
  • Antibodies may be used to bind to the liposome surface and to direct the antibody and its drug contents to specific antigenic receptors located on a particular cell-type surface.
  • Carbohydrate determinants may also be used as recognition sites as they have potential in directing liposomes to particular cell types. Usually, it is contemplated that intravenous injection of liposomal preparations would be used, but other routes of administration are also conceivable.
  • the invention provides for pharmaceutically-acceptable nanocapsule formulations of the compositions of the present invention.
  • Nanocapsules can generally entrap compounds in a stable and reproducible way (Henry-Michelland et al., 1987; Quintanar-Guerrero et al., 1998; Douglas et al., 1987).
  • ultra fine particles sized around 0.1 .mu.m
  • Biodegradable polyalkyl-cyanoacrylate nanoparticles that meet these requirements are contemplated for use in the present invention.
  • the subjects treated will typically comprise of mammals and will preferably be human subjects, e.g., human cancer subjects.
  • the compounds of the invention may be used alone or in combination. Additionally, the treated compounds may be utilized with other types of treatments, e.g., cancer treatments.
  • the subject compounds may be used with other chemotherapies, e.g., tamoxifen, taxol, methothrexate, biologicals, such as antibodies, growth factors, lymphokines, or radiation, etc. Combination therapies may result in synergistic results.
  • the preferred indication is cancer, especially the cancers identified previously.
  • compositions and methods provided herein are particularly deemed useful for the treatment of cancer including solid tumours such as skin, breast, brain, cervical carcinomas, testicular carcinomas, etc. More particularly, cancers that may be treated by the compositions and methods of the invention include, but are not limited to: Cardiac: sarcoma (angiosarcoma, fibrosarcoma, rhabdomyosarcoma, liposarcoma), myxoma, rhabdomyoma, fibroma, lipoma and teratoma; Lung: bronchogenic carcinoma (squamous cell, undifferentiated small cell, undifferentiated large cell, adenocarcinoma), alveolar (bronchiolar) carcinoma, bronchial adenoma, sarcoma, lymphoma, chondromatous hamartoma, mesotheliorna; Gastrointestinal: oesophagus (squamous cell carcinoma, adenocar
  • cancer refers to all types of cancer or neoplasm or malignant tumours found in mammals, including carcinomas and sarcomas.
  • examples of cancers are cancer of the brain, breast, cervix, colon, head & neck, kidney, lung, non-small cell lung, melanoma, mesothelioma, ovary, sarcoma, stomach, uterus and Medulloblastoma.
  • leukaemia refers broadly to progressive, malignant diseases of the blood-forming organs and is generally characterized by a distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukaemia is generally clinically classified on the basis of (1) the duration and character of the disease-acute or chronic; (2) the type of cell involved; myeloid (myelogenous), lymphoid (lymphogenous), or monocytic; and (3) the increase or non-increase in the number abnormal cells in the blood-leukaemic or aleukaemic (subleukaemic).
  • the P388 leukaemia model is widely accepted as being predictive of in vivo anti-leukaemic activity.
  • the present invention includes a method of treating leukaemia, and, preferably, a method of treating acute nonlymphocytic leukaemia, chronic lymphocytic leukaemia, acute granulocytic leukaemia, chronic granulocytic leukaemia, acute promyelocytic leukaemia, adult T-cell leukaemia, aleukaemic leukaemia, a leukocythemic leukaemia, basophylic leukaemia, blast cell leukaemia, bovine leukaemia, chronic myelocytic leukaemia, leukaemia cutis, embryonal leukaemia, eosinophilic leukaemia, Gross' leukaemia, hairy-cell leukaemia, hemoblastic leukaemia, hemocytoblastic leuk
  • sarcoma generally refers to a tumour which is made up of a substance like the embryonic connective tissue and is generally composed of closely packed cells embedded in a fibrillar or homogeneous substance.
  • Sarcomas which can be treated with combination-composition of the invention and optionally a potentiator and/or chemotherapeutic agent include a chondrosarcoma, fibrosarcoma, lymphosarcoma, melanosarcoma, myxosarcoma, osteosarcoma, Abemethy's sarcoma, adipose sarcoma, liposarcoma, alveolar soft part sarcoma, ameloblastic sarcoma, botryoid sarcoma, chloroma sarcoma, chorio carcinoma, embryonal sarcoma, Wilms' tumour sarcoma, endometrial sarcoma, stromal sarcoma, Ewing
  • melanoma is taken to mean a tumour arising from the melanocytic system of the skin and other organs.
  • Melanomas which can be treated with said combination-compositions and optionally a potentiator and/or another chemotherapeutic agent include acral-lentiginous melanoma, amelanotic melanoma, benign juvenile melanoma, Cloudman's melanoma, S91 melanoma, Harding-Passey melanoma, juvenile melanoma, lentigo maligna melanoma, malignant melanoma, nodular melanoma, subungal melanoma, and superficial spreading melanoma.
  • carcinoma refers to a malignant new growth made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases.
  • exemplary carcinomas which can be treated with said combination-compositions and optionally a potentiator and/or a chemotherapeutic agent include, for example, acinar carcinoma, acinous carcinoma, adenocystic carcinoma, adenoid cystic carcinoma, carcinoma adenomatosum, carcinoma of adrenal cortex, alveolar carcinoma, alveolar cell carcinoma, basal cell carcinoma, carcinoma basocellulare, basaloid carcinoma, basosquamous cell carcinoma, bronchioalveolar carcinoma, bronchiolar carcinoma, bronchogenic carcinoma, cerebriform carcinoma, cholangiocellular carcinoma, chorionic carcinoma, colloid carcinoma, comedo carcinoma, corpus carcinoma, cribriform carcinoma, carcinoma en cuirasse, carcinoma cutaneum, cylindrical carcinoma, cylindrical cell carcinoma, duct carcinoma, carcinoma durum, embryonal carcinoma, encephaloid carcinoma,
  • Additional cancers which can be treated with the composition according to the invention include, for example, Hodgkin's Disease, Non-Hodgkin's Lymphoma, multiple mycloma, neuroblastoma, breast cancer, ovarian cancer, lung cancer, rhabdomyosarcoma, primary thrombocytosis, primary macroglobulinemia, small-cell lung tumours, primary brain tumours, stomach cancer, colon cancer, malignant pancreatic insulanoma, malignant carcinoid, unary bladder cancer, pre-malignant skin lesions, testicular cancer, lymphomas, thyroid cancer, neuroblastoma, oesophageal cancer, genitourinary tract cancer, malignant hypercalcaemia, cervical cancer, endometrial cancer, adrenal cortical cancer, and prostate cancer.
  • the present invention concerns the use of proline or proline derivatives or their salts, esters, isomers or prodrugs to increase and/or optimise the binding of anti-cancer antibodies to the tumour antigens and/or cell receptors. Therefore a method of improving target selectivity of antibodies, wherein the target is treated in vitro or in vivo with the combination composition of the invention or with proline, proline derivatives or their salts, esters, isomers or prodrugs, is also an object of the present invention.
  • antibodies refers to the proteins produced by cells of the immune system which attach to certain chemicals that the body recognises as not being part of its own normal tissues. Antibodies help the body to resist infections and even cancer.
  • mAbs Monoclonal antibodies
  • trastuzumab Herceptin
  • Herceptin is the first monoclonal antibody drug used to treat women with breast cancer. It works by preventing the HER2/neu protein from promoting excessive growth of breast cancer cells and may also help the immune system fight the cancer.
  • monoclonal antibodies that recognise the HER2/neu protein are being tested in clinical trials as are monoclonal antibodies that block other growth-promoting molecules of breast cancer cells.
  • Monoclonal antibodies that have been designed to guide immune system cells, chemotherapy drugs, or radiation therapy directly to the tumour are also being tested.
  • Monoclonal antibodies bind to specific proteins which are found on the surface of human cells and play a role in the cell growth regulation, e.g. Herceptin binds to a protein called HER2.
  • Herceptin inhibited tumour cell growth by this binding action. In the case of metastatic breast cancer cells, approximately 80% of the tumours produce excess amounts of HER2.
  • the antibodies can be used either alone to kill cancer cells, or as carriers of other substances used also for treatment of diagnostic purposes.
  • chemotherapeutic agents can be attached to monoclonal antibodies to deliver high concentrations of these toxic substances directly to the tumour cells. In theory, this approach is less toxic and more effective than conventional chemotherapy because it reduces the delivery of harmful agents to normal tissues.
  • monoclonal antibodies may be used to carry radioactive substances to cancer cells within the body, thus pinpointing the location of metastases that were previously undetected by other methods.
  • the potential side effects of monoclonal antibodies may include dyspnoea (shortness of breathe) and mild wheezing, fever, headache, rash, nausea and vomiting, tachycardia (rapid heartbeat) and/or allergic reactions.
  • chemotherapeutics including cisplatin, carboplatin, taxol, 5FU etc, are highly toxic and generally poorly tolerated.
  • the potential side effects of chemotherapeutics may include haematologic toxicities such as thrombocytopenia, leucopoenia and anaemia, nonhaematologic toxicities such as nephrotoxicity, ototoxicity, neurotoxicity and emesis, injection site complications, sepsis, cardiovascular effects such as hypotension and bradycardia, diarrhoea, mucositis, dermatologic effects such as alopecia, respiratory effects such as interstitial pneumonia, lung fibrosis and pulmonary embolism, metabolic/nutritional effects such as weight loss, peripheral oedema and/or dehydration.
  • Cis-4-hydroxy-L-proline is a human endogenous compound with unknown physiological functions.
  • the trans-isomer of CHP is present in high concentrations in collagen and elastin, and therefore is vital for connective tissue synthesis and structure.
  • Endogenous concentrations of CHP have been determined in plasma and urine samples collected from healthy volunteers and cancer patients. Cancer patients treated with high doses of oral CHP have shown high concentrations of CHP and trans-4-hydroxy-L-proline (THP) in blood plasma. The results indicate that CHP and THP may have a relevant physiological role, which is not yet elucidated.
  • CHP 4-hydroxy-1-methyl-proline, 1-methyl-4-phenylamino-carbonyloxy-proline and other proline derivatives described above (which are the proline derivatives included in the present inventions idea and claims), may effect the cellular change, modification, generation and/or normalisation of the cell and/or may improve the agglutination behaviours of the tumour cells in a specific manner which may surprisingly result in an increase in the efficacy of the mAbs, and/or bispecific antibodies (bs-Abs) and/or other antibodies in targeting the specific tumour antigens such as EGFR's.
  • Proline, or proline derivatives or their salts, esters, isoforms or prodrugs can be administered in different schemes (prior, simultaneously or post) treatment with antibodies and/or pharmacological agents, drugs and any ingredients.
  • the agents described in the invention could be administered in any pharmaceutical formulation, e.g. infusion, injection, intramuscular, subcutaneous, etc.
  • Cis-4-hydroxy-1-proline (CHP) and a number of its derivatives have been investigated in combination with Cetuximab, Rituximab, Avastatin and specific EGFR-Antibodies against a panel of cancer cell lines.
  • MTT proliferation tests were performed as described.
  • the proliferation control of both the untreated cells and the CHP pre-treated cells is set to 100%.
  • optical density was measured at 450 nm using an empty well as reference in a microplate reader (Eurogenetics, Brussels, Belgium). For each cell line, 8 wells were used to measure the MTT signal of the medium control without test substances and the proliferation in the test wells was calculated in relation to these control values set to 100%. Test results were recorded between 0.3 and 1.5 optical densities for slowly and rapidly proliferating cells respectively.
  • A431 epidermoid carcinoma exhibits a pronounced overexpression of the epidermal growth factor receptor (EGFR; in our experiments approximately 20 ⁇ fold compared to the EGFR-positive colon cancer cell lines).
  • SW620con SW620chp4 Cetuximab ( ⁇ g/ml) 100.5 ⁇ 4.3 98.5 ⁇ 3.2 50 101.7 ⁇ 2.7 99.2 ⁇ 2.9 25 100.2 ⁇ 4.0 98.6 ⁇ 2.6 12.5 102.7 ⁇ 1.8 97.8 ⁇ 4.1* 6.3 101.8 ⁇ 2.1 92.7 ⁇ 0.6* 3.2 101.5 ⁇ 1.5 93.9 ⁇ 2.1* 1.6
  • SW620 EGFR-low expressing cell line pre-incubation with CHP surprisingly resulted in more inhibitory activity for Cetuximab at low concentrations (1.6-6.3 ⁇ g/ml).
  • A431 EGFR-overexpressing cell line pre-incubation of A431 cells with CHP (which reduced expression of EGFR) surprisingly results in antagonistic interaction with Cetuximab.
  • CHP is surprisingly antagonistic with Cetuximab for Colo205 cells at higher concentrations of CHP (50, 200 and 400 ⁇ g/ml) and surprisingly antagonistic with Cetuximab for SW620 cells at low concentrations of CHP (6.3-50 ⁇ g/ml).
  • Colo205 express significant amounts of EGFR at the cell surface, whereas SW620 seems to have very low expression of EGFR (data not shown).
  • HT29con HT29chp2 WI38con WI38chp2 96.9 ⁇ 1.1 101.6 ⁇ 2.2* 93.1 ⁇ 1.8 110.5 ⁇ 6.1* 100.3 ⁇ 2.4 102.5 ⁇ 4.6 91.8 ⁇ 3.8 118.8 ⁇ 10.1** 99.9 ⁇ 1.8 103.5 ⁇ 1.1 87.1 ⁇ 5.0 125.6 ⁇ 0.5* 100.4 ⁇ 4.4 104.5 ⁇ 3.7 84.1 ⁇ 0.5 116.0 ⁇ 2.5* 97.6 ⁇ 8.8 106.1 ⁇ 6.6 88.5 ⁇ 2.0 117.9 ⁇ 1.1* 96.6 ⁇ 7.3 90.1 ⁇ 3.8 94.7 ⁇ 0.9 116.5 ⁇ 7.4* DLD1con DLD1chp2 93.4 ⁇ 5.2 103.3 ⁇ 3.5* 99.8 ⁇ 0.2 108.7 ⁇ 15.1* 98.1 ⁇ 4.9 106.8 ⁇ 7.1 109.3 ⁇ 6.8 107.1 ⁇ 8.1 106.8 ⁇ 6.2 112.9
  • CHP is surprisingly antagonistic at low concentrations of CHP (5 and 2.5 ⁇ g/ml), whereas in other concentrations there was no significant interaction.
  • Colo 205 cells The sensitivity of Colo 205 cells to Cetuximab was tested following pre-incubation of the cells with the respective derivative (A1.21, A1.23 and A2.23) for 5 days in tissue culture (50 ⁇ g/ml).
  • Cells are expected to be CD20-negative. Surprisingly showed synergy with CHP for MIAPaCa2.

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CN1997365A (zh) 2007-07-11
BRPI0512040A (pt) 2008-02-06
WO2005120495A1 (en) 2005-12-22
US20050276810A1 (en) 2005-12-15
AU2005251463A1 (en) 2005-12-22
CA2568306A1 (en) 2005-12-22
EP1765328A1 (de) 2007-03-28
MXPA06014731A (es) 2007-04-25
KR20070026646A (ko) 2007-03-08
JP2008502622A (ja) 2008-01-31
ZA200700367B (en) 2008-07-30

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